JCV-specific T-cells producing IFN-gamma are differently associated with PmL occurrence in HIV patients and liver transplant recipients

Aim of this work was to investigate a possible correlation between the frequency of JCV-specific T-cells and PML occurrence in HIV-infected subjects and in liver transplant recipients. A significant decrease of JCV-specific T-cells was observed in HIV-PML subjects, highlighting a close relation between JCV-specific T-cell immune impairment and PML occurrence in HIV-subjects. Interestingly, liver-transplant recipients (LTR) showed a low frequency of JCV-specific T-cells, similar to HIV-PML subjects. Nevertheless, none of the enrolled LTR developed PML, suggesting the existence of different immunological mechanisms involved in the maintenance of a protective immune response in LT

Natural based products for cleaning copper and copper alloys artefacts

Copper alloys objects can deteriorate their conservation state through irreversible corrosion. Since in the cultural heritage field every artefact is unique and any loss irreplaceable, solutions for conservation are needed. Hence, there is the necessity to stop the corrosion process with a suitable cleaning and conservation process to avoid further degradation processes without changing its morphological aspect. Chelating solutions are commonly used in chemical cleaning, mainly sodium salts of ethylenediaminetetraacetic acid (EDTA). However, it is resistant to water purification procedures and is not biodegradable. The goal of this study was to see if applying an ecologically friendly chelating agent as an alternative to EDTA cleaning procedures for cultural heritage was suitable. In this study were chosen six natural-based chelators that could be a new green non-toxic alternative to EDTA in corrosion-inhibiting properties. They were tested for cleaning copper artefacts exposed to atmospheric environment in polluted areas. The study considered four amino acids, a glucoheptonate (CSA) and an industrial green chelator (GLDA). The effectiveness was tested on corrosion copper compounds and on laboratory corroded copper sheets. Finally, the cleaning efficacy was tested on four Roman coins and a modern copper painting. To define the cleaning efficacy, surface analytical investigations have been carried out by means ICP-OES, UV-VIS, µ-Raman, spectro-colorimetry, XRD and FTIR. Among the amino acids, alanine was the most effective, showing an unaltered noble patina and a good effective copper recovery from corrosion patinas

Bridging and downstaging to transplantation in HCC

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L-DOPA preloading increases the uptake of borophenylalanine in C6 glioma rat model: a new strategy to improve BNCT efficacy.

Purpose: Boron neutron capture therapy (BNCT) is a radiotherapeutic modality based on 10B(n,a)7Li reaction, for the treatment of malignant gliomas. One of the main limitations for BNCT effectiveness is the insufficient intake of 10B nuclei in the tumor cells. This work was aimed at investigating the use of L-DOPA as a putative enhancer for 10B-drug 4-dihydroxy-borylphenylalanine (BPA) uptake in the C6-glioma model. The investigation was first per- formed in vitro and then extended to the animal model. Methods and Materials: BPA accumulation in C6-glioma cells was assessed using radiowave dielectric spectros- copy, with and without L-DOPA preloading. Two L-DOPA incubation times (2 and 4 hours) were investigated, and the corresponding effects on BPA accumulation were quantified. C6-glioma cells were also implanted in the brain of 32 rats, and tumor growth was monitored by magnetic resonance imaging. Rats were assigned to two experimental branches: (1) BPA administration; (2) BPA administration after pretreatment with L-DOPA. All an- imals were sacrificed, and assessments of BPA concentrations in tumor tissue, normal brain, and blood samples were performed using high-performance liquid chromatography. Results: L-DOPA preloading induced a massive increase of BPA concentration in C6-glioma cells only after a 4-hour incubation. In the animal model, L-DOPA pretreatment produced a significantly higher accumulation of BPA in tumor tissue but not in normal brain and blood samples. Conclusions: This study suggests the potential use of L-DOPA as enhancer for BPA accumulation in malig- nant gliomas eligible for BNCT. L-DOPA preloading effect is discussed in terms of membrane transport mechanisms

Emergenza sismica nel Frusinate (Ottobre 2009 – Gennaio 2010): l’intervento della Rete Sismica Mobile stand-alone e l’analisi dati

Tra il 30 settembre ed il 22 ottobre del 2009 una piccola area della provincia di Frosinone, presso la località di Campoli Appennino, non lontana dalla città di Sora e dal confine con l’Abruzzo, è stata interessata da uno sciame sismico la cui fase più intensa è stata raggiunta nella notte tra il 7 e l’8 di ottobre con due scosse di magnitudo locale (ML) 3.6 e 3.4. Nei primi 23 giorni della sequenza (30 settembre – 22 ottobre) sono state registrate ben 1075 scosse, tutte con magnitudo non superiore a 3.6. In precedenza, nei mesi di maggio e giugno del 2009, si era attivata una piccola area posta ad una quindicina di chilometri a NW di Campoli Appennino, esattamente nella zona montuosa che separa la Val Roveto dalla Vallelonga in territorio abruzzese. Questo piccolo sciame è stato caratterizzato da 64 eventi con ML non superiore a 2.7. Diverse sono state le ragioni che hanno indotto il team scientifico alla guida della Rete Sismica Mobile della sede di Roma [Re.Mo., Moretti et al., 2010a] a disporre nei primi giorni del mese di ottobre un intervento di emergenza nell’area che include i comuni di Sora, Atina, San Donato in Val Comino e Pescasseroli tra le provincie di Frosinone e de L’Aquila: 1) la relativa vicinanza delle due zone epicentrali sopra descritte alla regione dell’Aquilano colpita solo pochi mesi prima dal forte evento sismico del 6 aprile 2009 (ML 5.8, MW 6.31) [Chiarabba et al., 2009; Margheriti et al., 2010], 2) l’emotività della popolazione originatasi a seguito del forte trauma vissuto e 3) non ultimo la psicosi collettiva notevolmente alimentata dai media locali e nazionali. In tutto, sono state installate 4 stazioni sismiche temporanee ad integrazione delle permanenti già presenti in area epicentrale al fine di migliorarne il monitoraggio. In questo lavoro viene presentato l’intervento della Re.Mo. riportando le motivazioni che lo hanno guidato e la tempistica delle operazioni svolte. Inoltre, verrà fornita una breve descrizione delle caratteristiche geologico-strutturali e sismotettoniche dell’area e saranno mostrate alcune analisi eseguite sui dati acquisiti in campagna

FRI0376 EFFECT OF CARBAMYLATED LOW-DENSITY LIPOPROTEINS ON BONE CELLS HOMEOSTASIS

Background:Carbamylation is a post-translational modification occurring under several conditions such as uremia, smoking and chronic inflammation as in rheumatoid arthritis (RA). Low-density lipoproteins (LDL) represent a target of carbamylation. Carbamylated-LDL (cLDL) have an increased inflammatory and atherogenic potential. Growing evidence supports an influence of modified lipids on bone cells homeostasis. However, the role of cLDL on bone cells physiology is still unknown.Objectives:Considering the rate of carbamylation and the role of anti-carbamylated proteins antibodies as markers of erosive disease in RA, the purpose of this study is to investigate the effect of cLDL on bone homeostasis.Methods:In-vitrocarbamylation of LDL was performed as previously described by Ok et al. (Kidney Int. 2005). Briefly, native LDL (nLDL) were treated with potassium cyanate (KOCN) for 4 hours, followed by excessive dialysis for 36 hours to remove KOCN. Both osteoclasts (OCs) and osteoblasts (OBLs) were treated at baseline with 20 μg/ml, 100 μg/ml and 200 μg/ml of cLDL or nLDL. To induce osteoclast differentiation, CD14+ monocytes were isolated from peripheral blood of healthy donors by magnetic microbeads separation and then cultured on a 96-wells plate in DMEM media supplemented with RANKL and M-CSF. After 10 days cells were fixed, stained for tartrate-resistant acid phosphatase (TRAP), a marker of OC differentiation, and counted. OBLs were isolated from bone specimens of 3 patients who had undergone to knee or hip arthroplasty for osteoarthritis and treated for 5 days with different concentrations of cLDL and nLDL. OBLs were fixed and stained for alkaline phosphatase positive activity (ALP), a marker of osteogenic differentiation. Total RNA was extracted from cell lysates. Copies of single-stranded complementary DNA (cDNA) were synthesized and analyzed by real-time PCR to evaluate RANKL and Osteoprotegerin (OPG) mRNA expression levels.Results:In OCLs culture, cLDL significantly decreased the number of OC compared to untreated cells (200 μg/ml p=0,0015) and nLDL treated cells (200 μg/ml p= 0,011; 20 μg/ml p= 0,0014) (Fig 1). Moreover, treatment with cLDL induced an increase of not terminally differentiated OCs, reduced dimensions of OCs, less intense TRAP staining and vacuolization (Fig 2). In OBLs culture, cLDL (20, 100 μg/ml) significantly reduced the ALP activity of OBLs compared with untreated cells (p<0.05) (Fig 3). nLDL did not affect the ALP expression. Treatment with cLDL stimulated RANKL mRNA expression in osteoblasts increasing the RANKL/OPG ratio (Fig 4).Fig 1.Fig 2.Fig 3.Fig 4.Conclusion:cLDL induce a significant depression of OC and OBL differentiation. Moreover, cLDL increase RANKL expression in OBL, unbalancing bone tissue turnover towards bone resorption. Accordingly, cLDL could be implicated in the bone loss characterizing several conditions associated to an increased carbamylation, such as RADisclosure of Interests:Bruno Lucchino: None declared, Martina Leopizzi: None declared, Tania Colasanti: None declared, Valeria Di Maio: None declared, cristiano alessandri Grant/research support from: Pfizer, Guido Valesini: None declared, fabrizio conti Speakers bureau: BMS, Lilly, Abbvie, Pfizer, Sanofi, Manuela Di Franco: None declared, Francesca Romana Spinelli Grant/research support from: Pfizer, Consultant of: Novartis, Gilead, Lilly, Sanofi, Celgene, Speakers bureau: Lill

La Rete Sismica Mobile del Centro Nazionale Terremoti

Il monitoraggio sismico e vulcanico del territorio nazionale rappresenta uno dei principali compiti istituzionali dell’Istituto Nazionale di Geofisica e Vulcanologia (INGV). L’INGV svolge tale importante funzione attraverso la gestione e la manutenzione di reti sismiche di diversa tipologia e a differente scala che consentono di monitorare il territorio nazionale in tempo reale. Tre sale di sorveglianza, una sismica presso la sede centrale di Roma e due vulcaniche presso la Sezione di Catania e l’Osservatorio Vesuviano di Napoli, con personale qualificato in turno H24, consentono di elaborare e comunicare tempestivamente al Dipartimento della Protezione Civile Nazionale (DPC) e alle sue strutture regionali eventuali stati di allarme e il livello dell’emergenza. Il Centro Nazionale Terremoti (CNT) è la sezione dell’INGV preposta al monitoraggio sismico del territorio italiano ed interviene in questo importante servizio attraverso la gestione e la manutenzione della Rete Sismica Nazionale (RSN) in collaborazione con le altre sedi dell’INGV dislocate sul territorio e con gli uffici tecnici locali. Competenza del CNT è anche la rete sismica euro-mediterranea (MedNet): una rete di stazioni sismiche a larga banda dislocate nei Paesi che circondano il Mediterraneo in condivisione con molti istituti geofisici. Negli ultimi anni tali reti sono cresciute sia come numero di stazioni che come tecnologia, consentendo di controllare in maniera estesa lo spettro di frequenze emesse dalla sorgente sismica e la ciclicità delle strutture sismogenetiche. In alcune aree del territorio nazionale l’alta densità di tali reti sismiche rende possibile una soglia di detezione degli eventi molto bassa e localizzazioni di elevata precisione che permettono di associare la micro-sismicità alle strutture sismo-genetiche. Tuttavia questo non è tecnicamente ed economicamente possibile in maniera omogenea su tutto il territorio nazionale. Per tale motivo si fa spesso ricorso all’uso di reti temporanee in esperimenti mirati allo studio di aree a peculiare rischio sismico e vulcanico o, in caso di forti terremoti, per aumentare la densità della rete già presente e migliorare il monitoraggio in real-time in modo tale da analizzare con maggior dettaglio l’evoluzione della sequenza. Unità specializzate nella gestione di reti sismologiche temporanee sono presenti in diverse sedi dell’INGV. Esse lavorano in completa autonomia sul territorio di competenza ma sono in grado di realizzare un buon livello di sinergia là dove esperimenti ed emergenze sismiche richiedano una stretta collaborazione. La struttura più grande, sia come numero di strumenti a disposizione (più di 200 tra digitalizzatori e sensori) che come personale impegnato, è la Rete Sismica Mobile (RSM) del CNT che è organizzata in modo da rendere possibile l’impiego della strumentazione in più esperimenti mantenendo una quota di strumenti riservata per gli interventi di emergenza. In questo rapporto tecnico presentiamo la struttura organizzativa ed operativa della RSM del CNT, la strumentazione in uso presso di essa e le diverse configurazioni possibili per le stazioni sismometriche temporanee con l’obiettivo di fornire un manuale d’uso ai ricercatori, tecnologi e tecnici che si interfacciano con la RSM, sia durante l’attività scientifica ordinaria (esperimenti di sismica passiva e attiva) che straordinaria (emergenze sismiche)

La campagna sismica del progetto “Alto Adriatico”. Rapporto delle attività 2010-2011

Istituto Nazionale di Geofisica e VulcanologiaPublished1-401.1. TTC - Monitoraggio sismico del territorio nazionaleN/A or not JCRope

Anti-D4GDI antibodies activate platelets in vitro. a possible link with thrombocytopenia in primary antiphospholipid syndrome

Background: Thrombocytopenia is a manifestation associated with primary antiphospholipid syndrome (PAPS), and many studies have stressed the leading role played by platelets in the pathogenesis of antiphospholipid syndrome (APS). Platelets are highly specialized cells, and their activation involves a series of rapid rearrangements of the actin cytoskeleton. Recently, we described the presence of autoantibodies against D4GDI (Rho GDP dissociation inhibitor beta, ARHGDIB) in the serum of a large subset of SLE patients, and we observed that anti-D4GDI antibodies activated the cytoskeleton remodeling of lymphocytes by inhibiting D4GDI and allowing the upregulation of Rho GTPases, such as Rac1. Proteomic and transcriptomic studies indicate that D4GDI is very abundant in platelets, and small GTPases of the RHO family are critical regulators of actin dynamics in platelets. Methods: We enrolled 38 PAPS patients, 15 patients carrying only antiphospholipid antibodies without clinical criteria of APS (aPL carriers) and 20 normal healthy subjects. Sera were stored at - 20 °C to perform an ELISA test to evaluate the presence of anti-D4GDI antibodies. Then, we purified autoantibodies anti-D4GDI from patient sera. These antibodies were used to conduct in vitro studies on platelet activation. Results: We identified anti-D4GDI antibodies in sera from 18/38 (47%) patients with PAPS, in sera from 2/15(13%) aPL carriers, but in no sera from normal healthy subjects. Our in vitro results showed a significant 30% increase in the activation of integrin αIIbβ3 upon stimulation of platelets from healthy donors preincubated with the antibody anti-D4GDI purified from the serum of APS patients. Conclusions: In conclusion, we show here that antibodies anti-D4GDI are present in the sera of PAPS patients and can prime platelet activation, explaining, at least in part, the pro-thrombotic state and the thrombocytopenia of PAPS patients. These findings may lead to improved diagnosis and treatment of APS